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Bifunctional enzyme deficiency
Bifunctional enzyme deficiency
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
BIFUNCTIONAL ENZYME DEFICIENCY
300
EHHADH
Unknown
9501266
Orphanet
Fatty acid degradation
Valine, leucine and isoleucine degradation
Lysine degradation
Tryptophan metabolism
beta-Alanine metabolism
Propanoate metabolism
Butanoate metabolism
Metabolic pathways
Fatty acid metabolism
PPAR signaling pathway
Peroxisome
Beta-oxidation of very long chain fatty acids
Peroxisomal protein import
+10 more
HSD17B4
Unknown
24553428
25967389
9915948
Orphanet
Primary bile acid biosynthesis
Biosynthesis of unsaturated fatty acids
Metabolic pathways
Fatty acid metabolism
Peroxisome
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
alpha-linolenic acid (ALA) metabolism
Beta-oxidation of pristanoyl-CoA
Beta-oxidation of very long chain fatty acids
Peroxisomal protein import
+7 more
All
2
Causal
1
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
2
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Bifunctional enzyme deficiency.
5
View disease cluster →
D-bifunctional protein deficiency
1 shared gene
HSD17B4
Related via 1 shared gene including HSD17B4.
Fatty acid metabolism disorder
1 shared gene
HSD17B4
Related via 1 shared gene including HSD17B4.
De toni-debre-fanconi syndrome
1 shared gene
EHHADH
Related via 1 shared gene including EHHADH.
Fanconi renotubular syndrome
1 shared gene
EHHADH
Related via 1 shared gene including EHHADH.
Peroxisomal disorder
1 shared gene
HSD17B4
Related via 1 shared gene including HSD17B4.
1
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